批准日期,申请提交历史,通知信,药品说明书,审评文件等信息
提交状态日期 | 提交号 | 审批结论 | 申请内容分类 | 审评优先级;罕用药状态 | 通知信、审评文件、说明书、包装标签 | 备注 |
2022/11/09 |
SUPPL-26(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2022/11/09 |
SUPPL-23(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2018/03/14 |
SUPPL-15(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2017/03/24 |
SUPPL-14(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2017/03/24 |
SUPPL-13(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2016/02/28 |
SUPPL-10(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2013/10/07 |
SUPPL-7(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2013/04/26 |
SUPPL-6(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2008/06/18 |
SUPPL-2(补充) |
Approval |
Labeling |
|
|
|
2007/08/02 |
ORIG-1(原始申请) |
Approval |
|
|
|
|
与本品相关的专利信息(来自FDA橙皮书Orange Book)
关联产品号 | 专利号 | 专利过期日 | 是否物质专利 | 是否产品专利 | 专利用途代码 | 撤销请求 | 提交日期 | 专利下载 | 备注 |
无 |
与本品治疗等效的药品
活性成分:ONDANSETRON 剂型/给药途径:TABLET, ORALLY DISINTEGRATING;ORAL 规格:4MG 治疗等效代码:AB
申请号 | 产品号 | 申请类型 | 商品名 | 活性成分 | 剂型/给药途径 | 规格 | 市场状态 | RLD | RS | TE Code | 产品号批准日期 | 申请人 |
077406 |
003 |
ANDA |
ONDANSETRON |
ONDANSETRON |
TABLET, ORALLY DISINTEGRATING;ORAL |
4MG |
Prescription |
No |
No |
AB |
2006/12/26
|
CHARTWELL MOLECULES |
078139 |
001 |
ANDA |
ONDANSETRON |
ONDANSETRON |
TABLET, ORALLY DISINTEGRATING;ORAL |
4MG |
Discontinued |
No |
No |
AB |
2007/06/25
|
MYLAN |
078152 |
001 |
ANDA |
ONDANSETRON |
ONDANSETRON |
TABLET, ORALLY DISINTEGRATING;ORAL |
4MG |
Prescription |
No |
No |
AB |
2007/06/27
|
GLENMARK PHARMS LTD |
077557 |
001 |
ANDA |
ONDANSETRON |
ONDANSETRON |
TABLET, ORALLY DISINTEGRATING;ORAL |
4MG |
Prescription |
No |
No |
AB |
2007/08/02
|
SUN PHARM INDS |
078050 |
001 |
ANDA |
ONDANSETRON |
ONDANSETRON |
TABLET, ORALLY DISINTEGRATING;ORAL |
4MG |
Prescription |
No |
No |
AB |
2007/08/13
|
SANDOZ |
090469 |
001 |
ANDA |
ONDANSETRON |
ONDANSETRON |
TABLET, ORALLY DISINTEGRATING;ORAL |
4MG |
Prescription |
No |
No |
AB |
2010/04/12
|
AUROBINDO PHARMA |
078602 |
001 |
ANDA |
ONDANSETRON |
ONDANSETRON |
TABLET, ORALLY DISINTEGRATING;ORAL |
4MG |
Discontinued |
No |
No |
AB |
2011/02/24
|
SUN PHARM INDS LTD |
209389 |
001 |
ANDA |
ONDANSETRON |
ONDANSETRON |
TABLET, ORALLY DISINTEGRATING;ORAL |
4MG |
Prescription |
No |
No |
AB |
2023/10/30
|
IPCA LABS LTD |
活性成分:ONDANSETRON 剂型/给药途径:TABLET, ORALLY DISINTEGRATING;ORAL 规格:8MG 治疗等效代码:AB
申请号 | 产品号 | 申请类型 | 商品名 | 活性成分 | 剂型/给药途径 | 规格 | 市场状态 | RLD | RS | TE Code | 产品号批准日期 | 申请人 |
077406 |
004 |
ANDA |
ONDANSETRON |
ONDANSETRON |
TABLET, ORALLY DISINTEGRATING;ORAL |
8MG |
Prescription |
No |
No |
AB |
2006/12/26
|
CHARTWELL MOLECULES |
078139 |
002 |
ANDA |
ONDANSETRON |
ONDANSETRON |
TABLET, ORALLY DISINTEGRATING;ORAL |
8MG |
Discontinued |
No |
No |
AB |
2007/06/25
|
MYLAN |
078152 |
002 |
ANDA |
ONDANSETRON |
ONDANSETRON |
TABLET, ORALLY DISINTEGRATING;ORAL |
8MG |
Prescription |
No |
No |
AB |
2007/06/27
|
GLENMARK PHARMS LTD |
077557 |
002 |
ANDA |
ONDANSETRON |
ONDANSETRON |
TABLET, ORALLY DISINTEGRATING;ORAL |
8MG |
Prescription |
No |
No |
AB |
2007/08/02
|
SUN PHARM INDS |
078050 |
002 |
ANDA |
ONDANSETRON |
ONDANSETRON |
TABLET, ORALLY DISINTEGRATING;ORAL |
8MG |
Prescription |
No |
No |
AB |
2007/08/13
|
SANDOZ |
090469 |
002 |
ANDA |
ONDANSETRON |
ONDANSETRON |
TABLET, ORALLY DISINTEGRATING;ORAL |
8MG |
Prescription |
No |
Yes |
AB |
2010/04/12
|
AUROBINDO PHARMA |
078602 |
002 |
ANDA |
ONDANSETRON |
ONDANSETRON |
TABLET, ORALLY DISINTEGRATING;ORAL |
8MG |
Discontinued |
No |
No |
AB |
2011/02/24
|
SUN PHARM INDS LTD |
209389 |
002 |
ANDA |
ONDANSETRON |
ONDANSETRON |
TABLET, ORALLY DISINTEGRATING;ORAL |
8MG |
Prescription |
No |
No |
AB |
2023/10/30
|
IPCA LABS LTD |